Teclistamab in Previously Treated AL Amyloidosis

Sponsor
Peking Union Medical College Hospital
Study ID
NCT06935162
Phase
PHASE2
Status
Recruiting
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Conditions

  • AL Amyloidosis

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Teclistamab (Tec) — DRUG
    Teclistamab will be administered via a subcutaneous injection

Study Details

This is a phase II study in patients with previously treated immunoglobulin light-chain (AL) Amyloidosis to evaluate the efficacy and safety of teclistamab

Key Dates

Start date
May 21, 2025
Status verified
Apr 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2028

Study Design

Enrollment
30 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Teclistamab
    Teclistamab will be administered via a subcutaneous injection

Primary Outcome Measure

Hematologic complete response (CR) at 3 months after treatment initiation [ Time Frame: at 3 months after treatment initiation ]

Central Contacts

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